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FDA 510(k)

CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING

K-Number: K851382 · 1985-07-05

Decision Date1985-07-05
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. It received FDA 510(k) clearance on 1985-07-05 under 510(k) number K851382. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING?

CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1985-07-05. The listed applicant is Chesebrough-Pond'S U.S.A. Co.. The 510(k) number is K851382.

When did CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING receive FDA 510(k) clearance?

CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING received FDA 510(k) clearance on 1985-07-05, under 510(k) number K851382.

Who is the listed applicant for CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING?

The FDA 510(k) record lists Chesebrough-Pond'S U.S.A. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING?

The FDA product code for CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING is NAD.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Chesebrough-Pond'S U.S.A. Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 33 devices →

Related Devices (Code: NAD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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